Canonical Allele Identifier: CA2355189550
Gene: LINC01432 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069865A>T , CM000682.2:g.22069865A>T GRCh38
NC_000020.10:g.22050503A>T , CM000682.1:g.22050503A>T GRCh37
NC_000020.9:g.21998503A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1177A>T